ClinVar for Gene (Select 4635) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2862213	NM_002476.2(MYL4):c.487+3A>T	MYL4	Single nucleotide variant (intron variant)	Atrial fibrillation, familial, 18	GUncertain significance
Select item 2851150	NM_002476.2(MYL4):c.469C>G (p.His157Asp)	MYL4 (H157D)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 18	GUncertain significance
Select item 2842835	NM_002476.2(MYL4):c.175G>T (p.Ala59Ser)	MYL4 (A59S)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 18	GUncertain significance
Select item 2829405	NM_002476.2(MYL4):c.236G>A (p.Gly79Glu)	MYL4 (G79E)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 18	GUncertain significance
Select item 2828641	NM_002476.2(MYL4):c.196A>C (p.Thr66Pro)	MYL4 (T66P)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 18	GUncertain significance
Select item 2817467	NM_002476.2(MYL4):c.135+14A>G	MYL4	Single nucleotide variant (intron variant)	Atrial fibrillation, familial, 18	GLikely benign
Select item 2812561	NM_002476.2(MYL4):c.207A>T (p.Gly69=)	MYL4	Single nucleotide variant (synonymous variant)	Atrial fibrillation, familial, 18	GLikely benign
Select item 2768617	NM_002476.2(MYL4):c.70G>T (p.Ala24Ser)	MYL4 (A24S)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 18	GUncertain significance
Select item 2758813	NM_002476.2(MYL4):c.150C>G (p.Ala50=)	MYL4	Single nucleotide variant (synonymous variant)	Atrial fibrillation, familial, 18	GLikely benign
Select item 2740053	NM_002476.2(MYL4):c.235G>A (p.Gly79Arg)	MYL4 (G79R)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 18	GUncertain significance
Select item 2734686	NM_002476.2(MYL4):c.66C>T (p.Ala22=)	MYL4	Single nucleotide variant (synonymous variant)	Atrial fibrillation, familial, 18	GLikely benign
Select item 2731438	NM_002476.2(MYL4):c.60_71del (p.16AP[6])	MYL4	Deletion (inframe_deletion)	Atrial fibrillation, familial, 18	GUncertain significance
Select item 2711488	NM_002476.2(MYL4):c.565+4T>C	MYL4	Single nucleotide variant (intron variant)	Atrial fibrillation, familial, 18	GUncertain significance
Select item 2709227	NM_002476.2(MYL4):c.371C>T (p.Ser124Phe)	MYL4 (S124F)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 18	GUncertain significance
Select item 2706776	NM_002476.2(MYL4):c.230A>G (p.Gln77Arg)	MYL4 (Q77R)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 18	GUncertain significance
Select item 2706232	NM_002476.2(MYL4):c.481A>T (p.Thr161Ser)	MYL4 (T161S)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 18	GUncertain significance
Select item 2699912	NM_002476.2(MYL4):c.588A>G (p.Ser196=)	MYL4	Single nucleotide variant (synonymous variant)	Atrial fibrillation, familial, 18	GLikely benign
Select item 2635232	NM_002476.2(MYL4):c.376A>G (p.Asn126Asp)	MYL4 (N126D)	Single nucleotide variant (missense variant)	MYL4-related disorder	GUncertain significance
Select item 2622218	NM_002476.2(MYL4):c.25A>G (p.Lys9Glu)	MYL4 (K9E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2534904	NM_002476.2(MYL4):c.129T>A (p.Ser43Arg)	MYL4 (S43R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2506553	GRCh37/hg19 17q21.32(chr17:44949883-46507482)	CBX1, CDC27 +24 more	Copy number gain	PNPO-related disorder	GLikely pathogenic
Select item 2428375	NM_002476.2(MYL4):c.316A>G (p.Met106Val)	MYL4 (M106V)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 18	GUncertain significance
Select item 2418791	NM_002476.2(MYL4):c.200C>T (p.Pro67Leu)	MYL4 (P67L)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 18	GUncertain significance
Select item 2197754	NM_002476.2(MYL4):c.78_89dup (p.Pro31_Glu32insAlaProAlaPro)	MYL4	Duplication (inframe_insertion)	Atrial fibrillation, familial, 18	GUncertain significance
Select item 2196611	NM_002476.2(MYL4):c.370T>G (p.Ser124Ala)	MYL4 (S124A)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 18	GUncertain significance
Select item 2196342	NM_002476.2(MYL4):c.163+17C>A	MYL4	Single nucleotide variant (intron variant)	Atrial fibrillation, familial, 18	GLikely benign
Select item 2195755	NM_002476.2(MYL4):c.455G>A (p.Gly152Asp)	MYL4 (G152D)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 18	GUncertain significance
Select item 2186195	NM_002476.2(MYL4):c.193C>T (p.Arg65Trp)	MYL4 (R65W)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 18	GUncertain significance
Select item 2182397	NM_002476.2(MYL4):c.203C>T (p.Thr68Ile)	MYL4 (T68I)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 18	GUncertain significance
Select item 2165639	NM_002476.2(MYL4):c.361C>T (p.Gln121Ter)	MYL4 (Q121*)	Single nucleotide variant (nonsense)	Atrial fibrillation, familial, 18	GPathogenic
Select item 2164326	NM_002476.2(MYL4):c.441T>C (p.Asn147=)	MYL4	Single nucleotide variant (synonymous variant)	Atrial fibrillation, familial, 18	GLikely benign
Select item 2159572	NM_002476.2(MYL4):c.549C>T (p.Gly183=)	MYL4	Single nucleotide variant (synonymous variant)	Atrial fibrillation, familial, 18	GLikely benign
Select item 2155068	NM_002476.2(MYL4):c.317T>C (p.Met106Thr)	MYL4 (M106T)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 18	GUncertain significance
Select item 2153473	NM_002476.2(MYL4):c.225C>T (p.Tyr75=)	MYL4	Single nucleotide variant (synonymous variant)	Atrial fibrillation, familial, 18	GLikely benign
Select item 2147045	NM_002476.2(MYL4):c.135+1G>A	MYL4	Single nucleotide variant (splice donor variant)	Atrial fibrillation, familial, 18	GLikely pathogenic
Select item 2133442	NM_002476.2(MYL4):c.313+19C>T	MYL4	Single nucleotide variant (intron variant)	Atrial fibrillation, familial, 18	GLikely benign
Select item 2124518	NM_002476.2(MYL4):c.164-16G>A	MYL4	Single nucleotide variant (intron variant)	Atrial fibrillation, familial, 18	GLikely benign
Select item 2121055	NM_002476.2(MYL4):c.163+6T>A	MYL4	Single nucleotide variant (intron variant)	Atrial fibrillation, familial, 18	GUncertain significance
Select item 2090713	NM_002476.2(MYL4):c.313+1G>T	MYL4	Single nucleotide variant (splice donor variant)	Atrial fibrillation, familial, 18	GLikely pathogenic
Select item 2089894	NM_002476.2(MYL4):c.136-3C>T	MYL4	Single nucleotide variant (intron variant)	Atrial fibrillation, familial, 18	GUncertain significance
Select item 2071302	NM_002476.2(MYL4):c.19G>A (p.Glu7Lys)	MYL4 (E7K)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 18	GUncertain significance
Select item 2069664	NM_002476.2(MYL4):c.314-9T>C	MYL4	Single nucleotide variant (intron variant)	Atrial fibrillation, familial, 18	GLikely benign
Select item 2065572	NM_002476.2(MYL4):c.233G>A (p.Cys78Tyr)	MYL4 (C78Y)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 18	GUncertain significance
Select item 2065442	NM_002476.2(MYL4):c.467G>A (p.Arg156Gln)	MYL4 (R156Q)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2053340	NM_002476.2(MYL4):c.532C>T (p.Gln178Ter)	MYL4 (Q178*)	Single nucleotide variant (nonsense)	Atrial fibrillation, familial, 18	GPathogenic
Select item 2052621	NM_002476.2(MYL4):c.314-1G>C	MYL4	Single nucleotide variant (splice acceptor variant)	Atrial fibrillation, familial, 18	GLikely pathogenic
Select item 2049700	NM_002476.2(MYL4):c.253C>G (p.Leu85Val)	MYL4 (L85V)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 18	GUncertain significance
Select item 2029520	NM_002476.2(MYL4):c.291G>T (p.Val97=)	MYL4	Single nucleotide variant (synonymous variant)	Atrial fibrillation, familial, 18	GLikely benign
Select item 2023975	NM_002476.2(MYL4):c.565+12C>A	MYL4	Single nucleotide variant (intron variant)	Atrial fibrillation, familial, 18	GLikely benign
Select item 2018865	NM_002476.2(MYL4):c.102C>T (p.Pro34=)	MYL4	Single nucleotide variant (synonymous variant)	Atrial fibrillation, familial, 18	GLikely benign
Select item 2018006	NM_002476.2(MYL4):c.348C>T (p.Phe116=)	MYL4	Single nucleotide variant (synonymous variant)	Atrial fibrillation, familial, 18	GLikely benign
Select item 1997181	NM_002476.2(MYL4):c.103A>G (p.Lys35Glu)	MYL4 (K35E)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 18	GUncertain significance
Select item 1990377	NM_002476.2(MYL4):c.6T>C (p.Ala2=)	MYL4	Single nucleotide variant (synonymous variant)	Atrial fibrillation, familial, 18	GLikely benign
Select item 1983559	NM_002476.2(MYL4):c.125A>G (p.Lys42Arg)	MYL4 (K42R)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 18	GUncertain significance
Select item 1966224	NM_002476.2(MYL4):c.583A>G (p.Met195Val)	MYL4 (M195V)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 18	GUncertain significance
Select item 1955141	NM_002476.2(MYL4):c.504G>A (p.Glu168=)	MYL4	Single nucleotide variant (synonymous variant)	Atrial fibrillation, familial, 18	GLikely benign
Select item 1945778	NM_002476.2(MYL4):c.48TCCAGC[1] (p.16AP[6])	MYL4	Microsatellite (inframe_deletion)	Atrial fibrillation, familial, 18	GUncertain significance
Select item 1934923	NM_002476.2(MYL4):c.472G>A (p.Val158Ile)	MYL4 (V158I)	Single nucleotide variant (missense variant)	not specified +2 more	GUncertain significance
Select item 1933219	NM_002476.2(MYL4):c.315G>A (p.Glu105=)	MYL4	Single nucleotide variant (synonymous variant)	Atrial fibrillation, familial, 18	GLikely benign
Select item 1926635	NM_002476.2(MYL4):c.163+16C>T	MYL4	Single nucleotide variant (intron variant)	Atrial fibrillation, familial, 18	GLikely benign
Select item 1913187	NM_002476.2(MYL4):c.284T>C (p.Leu95Pro)	MYL4 (L95P)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 18	GUncertain significance
Select item 1905815	NM_002476.2(MYL4):c.314-16C>T	MYL4	Single nucleotide variant (intron variant)	Atrial fibrillation, familial, 18	GLikely benign
Select item 1672523	NM_002476.2(MYL4):c.300G>A (p.Lys100=)	MYL4	Single nucleotide variant (synonymous variant)	Atrial fibrillation, familial, 18	GLikely benign
Select item 1670009	NM_002476.2(MYL4):c.487+13G>A	MYL4	Single nucleotide variant (intron variant)	Atrial fibrillation, familial, 18	GLikely benign
Select item 1668883	NM_002476.2(MYL4):c.164-4A>C	MYL4	Single nucleotide variant (intron variant)	Atrial fibrillation, familial, 18	GLikely benign
Select item 1659289	NM_002476.2(MYL4):c.487+20A>C	MYL4	Single nucleotide variant (intron variant)	Atrial fibrillation, familial, 18	GLikely benign
Select item 1658308	NM_002476.2(MYL4):c.565+17T>C	MYL4	Single nucleotide variant (intron variant)	Atrial fibrillation, familial, 18	GLikely benign
Select item 1657579	NM_002476.2(MYL4):c.565+12C>T	MYL4	Single nucleotide variant (intron variant)	Atrial fibrillation, familial, 18	GLikely benign
Select item 1651475	NM_002476.2(MYL4):c.72A>C (p.Ala24=)	MYL4	Single nucleotide variant (synonymous variant)	Atrial fibrillation, familial, 18	GLikely benign
Select item 1631428	NM_002476.2(MYL4):c.487+14G>A	MYL4	Single nucleotide variant (intron variant)	Atrial fibrillation, familial, 18	GLikely benign
Select item 1624746	NM_002476.2(MYL4):c.565+10C>T	MYL4	Single nucleotide variant (intron variant)	Atrial fibrillation, familial, 18	GLikely benign
Select item 1623214	NM_002476.2(MYL4):c.234C>T (p.Cys78=)	MYL4	Single nucleotide variant (synonymous variant)	Atrial fibrillation, familial, 18	GLikely benign
Select item 1608185	NM_002476.2(MYL4):c.474C>T (p.Val158=)	MYL4	Single nucleotide variant (synonymous variant)	Atrial fibrillation, familial, 18	GLikely benign
Select item 1584783	NM_002476.2(MYL4):c.313+9G>A	MYL4	Single nucleotide variant (intron variant)	Atrial fibrillation, familial, 18	GLikely benign
Select item 1583500	NM_002476.2(MYL4):c.565+11G>A	MYL4	Single nucleotide variant (intron variant)	Atrial fibrillation, familial, 18	GBenign
Select item 1574879	NM_002476.2(MYL4):c.164-13C>G	MYL4	Single nucleotide variant (intron variant)	Atrial fibrillation, familial, 18	GLikely benign
Select item 1573458	NM_002476.2(MYL4):c.313+16T>C	MYL4	Single nucleotide variant (intron variant)	Atrial fibrillation, familial, 18	GLikely benign
Select item 1562996	NM_002476.2(MYL4):c.565+13G>A	MYL4	Single nucleotide variant (intron variant)	Atrial fibrillation, familial, 18	GLikely benign
Select item 1543806	NM_002476.2(MYL4):c.314-6C>T	MYL4	Single nucleotide variant (intron variant)	Atrial fibrillation, familial, 18	GLikely benign
Select item 1531208	NM_002476.2(MYL4):c.565+19C>T	MYL4	Single nucleotide variant (intron variant)	Atrial fibrillation, familial, 18	GLikely benign
Select item 1523169	NM_002476.2(MYL4):c.551G>A (p.Cys184Tyr)	MYL4 (C184Y)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 18	GUncertain significance
Select item 1515616	NM_002476.2(MYL4):c.392C>T (p.Thr131Ile)	MYL4 (T131I)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 18	GUncertain significance
Select item 1510596	NM_002476.2(MYL4):c.482C>T (p.Thr161Ile)	MYL4 (T161I)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 18	GUncertain significance
Select item 1509929	NM_002476.2(MYL4):c.14A>G (p.Lys5Arg)	MYL4 (K5R)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 18	GUncertain significance
Select item 1504263	NM_002476.2(MYL4):c.587C>G (p.Ser196Ter)	MYL4 (S196*)	Single nucleotide variant (nonsense)	Atrial fibrillation, familial, 18	GUncertain significance
Select item 1504023	NM_002476.2(MYL4):c.136A>T (p.Ile46Leu)	MYL4 (I46L)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 18	GUncertain significance
Select item 1500746	NM_002476.2(MYL4):c.199C>T (p.Pro67Ser)	MYL4 (P67S)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 18	GUncertain significance
Select item 1498777	NM_002476.2(MYL4):c.232T>C (p.Cys78Arg)	MYL4 (C78R)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 18 +1 more	GUncertain significance
Select item 1494319	NM_002476.2(MYL4):c.479C>T (p.Ala160Val)	MYL4 (A160V)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 18	GUncertain significance
Select item 1492672	NM_002476.2(MYL4):c.584T>C (p.Met195Thr)	MYL4 (M195T)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 18	GUncertain significance
Select item 1474944	NM_002476.2(MYL4):c.487+1G>A	MYL4	Single nucleotide variant (splice donor variant)	Atrial fibrillation, familial, 18	GLikely pathogenic
Select item 1468573	NM_002476.2(MYL4):c.248G>A (p.Arg83Gln)	MYL4 (R83Q)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 18	GUncertain significance
Select item 1461155	NM_002476.2(MYL4):c.223T>A (p.Tyr75Asn)	MYL4 (Y75N)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 18	GUncertain significance
Select item 1456150	NM_002476.2(MYL4):c.57A>G (p.Pro19=)	MYL4	Single nucleotide variant (synonymous variant)	Atrial fibrillation, familial, 18	GLikely benign
Select item 1449264	NM_002476.2(MYL4):c.373C>T (p.Arg125Cys)	MYL4 (R125C)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 18	GUncertain significance
Select item 1447947	NM_002476.2(MYL4):c.518A>G (p.Gln173Arg)	MYL4 (Q173R)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 18	GUncertain significance
Select item 1433563	NM_002476.2(MYL4):c.581T>C (p.Ile194Thr)	MYL4 (I194T)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 18	GUncertain significance
Select item 1430788	NM_002476.2(MYL4):c.234del (p.Cys78fs)	MYL4 (C78fs)	Deletion (frameshift variant)	Atrial fibrillation, familial, 18	GPathogenic
Select item 1427245	NM_002476.2(MYL4):c.38C>T (p.Ala13Val)	MYL4 (A13V)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 18	GUncertain significance
Select item 1391944	NM_002476.2(MYL4):c.530G>A (p.Gly177Glu)	MYL4 (G177E)	Single nucleotide variant (missense variant)	Atrial fibrillation, familial, 18	GUncertain significance

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